A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979483



Internal ID20546523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110025268..110037941hg38UCSC Ensembl
chr10:111785026..111797699hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3812674
hg1912674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454377
Supporting Variants
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00064


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